{
  "id": 10702,
  "label": "atresia of small intestine",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009476",
  "properties": {
    "xrefs": [
      "GARD:0000140",
      "MEDGEN:78590",
      "MESH:C538260",
      "MedDRA:10010626",
      "NCIT:C98828",
      "NORD:1309",
      "OMIM:243600",
      "Orphanet:1201",
      "UMLS:C0266172",
      "icd11.foundation:1949256262"
    ],
    "synonyms": [
      "Jejunal Atresia",
      "Jejunoileal atresia",
      "apple peel syndrome",
      "atresia of the small intestine",
      "congenital small intestine atresia",
      "intestinal atresia type IIIb",
      "jejunal atresia",
      "small intestinal atresia",
      "small intestine atresia",
      "APSB",
      "apple peel small bowel syndrome",
      "apple-peel intestinal atresia",
      "congenital atresia of the small intestine",
      "familial apple peel jejunal atresia"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "Atresia of small intestine is a special form of intestinal atresia with absence of mesentery, which is most likely due to an intrauterine intestinal vascular accident. Newborns are usually preterm infants with low birth-weights, that encounter feeding difficulties (including vomiting with initial feeds, which may later worsened and the abdomen becomes progressively distended) as well as failure to thrive. Affected children present disrupted bowel loops assuming a spiral configuration resembling an 'apple peel' and may have less than half of the normal length of the small bowel and a physiologically short bowel. Atresia of small intestine is characterized by jejunal atresia near the ligament of Treitz, foreshortened bowel, and a large mesenteric gap. The bowel distal to the atresia is precariously supplied. Atresia of small intestine may be a manifestation of cystic fibrosis. The most important cause of mortality is short bowel syndrome, encountered in 65% of cases."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:Q00-Q99",
          "MEDGEN:1843482",
          "UMLS:C0694457"
        ],
        "definition": "Any disease or disorder that disrupts the process development of an anatomical structure. Can be due to genetic or environmental causes. Typically happens during embryogenesis, but also includes post-embryonic development."
      },
      "child_count": 190,
      "reference_id": "MONDO:0021147"
    },
    {
      "id": 21546,
      "label": "small intestine disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:574283",
          "SCTID:119522002",
          "UMLS:C0341268"
        ],
        "synonyms": [
          "disease of small intestine",
          "disease or disorder of small intestine",
          "disorder of small intestine",
          "small intestine disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A disease that involves the small intestine."
      },
      "child_count": 10,
      "reference_id": "MONDO:0024635"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis"
    },
    {
      "id": 21546,
      "label": "small intestine disorder"
    }
  ]
}